Hybio Pharmaceutical Co., Ltd.
FDA inspection history in Shenzhen, China, 2015
- 1
- Form 483
Every document, by year
- Form 483
2015: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2015One Form 483, at Shenzhen, China.
Cited most
Across all Hybio Pharmaceutical Co. observations on file
- 21 CFR 211.160General requirements1
- 21 CFR 211.28Personnel responsibilities1
- 21 CFR 211.46Ventilation, air filtration, air heating and cooling1
- 21 CFR 211.67Equipment cleaning and maintenance1
The complete Hybio Pharmaceutical Co. file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Shenzhen, China
One Form 483 · 2015
Latest: Form 483, Jun 26, 2015 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2015-06-26 | 483 Form 483 | Shenzhen, China | — | $99 |
Investigators on these documents
FEI number 3010165930 · most recent document Jun 26, 2015
About Hybio Pharmaceutical Co., Ltd.
How many FDA Form 483s has Hybio Pharmaceutical Co., Ltd. received?
FDA Intel has 1 Form 483 on file for Hybio Pharmaceutical Co., Ltd.; the most recent is dated Jun 26, 2015.
When was Hybio Pharmaceutical Co., Ltd. last inspected by FDA?
The most recent FDA inspection document on file for Hybio Pharmaceutical Co., Ltd. is a Form 483 dated Jun 26, 2015, for the site in Shenzhen, China.
What did FDA cite at Hybio Pharmaceutical Co., Ltd.?
The regulations cited most in the observations on file for Hybio Pharmaceutical Co., Ltd. are 21 CFR 211.160 (General requirements), 1 time; 21 CFR 211.28 (Personnel responsibilities), 1 time; 21 CFR 211.46 (Ventilation, air filtration, air heating and cooling), 1 time.